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Vanguard™ Knee System

FDA UDI

Class I (US FDA UDI)

by Biomet Uk Ltd

Identity

Trade Name
Vanguard™ Knee System FDA UDI
Generic Name
Arthrodesis nail, non-sterile FDA UDI
Model / Reference
32-422623 FDA UDI

Identifiers

Catalog Number
32-422623 FDA UDI
Primary DI / UDI-DI
00887868526589 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Arthrodesis nail, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Arthrodesis nail, non-sterile

Vanguard™ Knee System by Biomet Uk Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthrodesis nail, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Uk Ltd

Sources (1)

  • FDA UDI 27b7f440-5a11-4d79-98fe-998a3ff61f42 34 fields · synced May 30, 2026